Canonical Allele Identifier: CA383505788

Gene: VWF

Linked Data

• gnomAD v4: 12-6019409-G-A
• MyVariant Identifiers: chr12:g.6128575G>A (hg19) ; chr12:g.6019409G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6019409G>A , CM000674.2:g.6019409G>A	GRCh38
NC_000012.11:g.6128575G>A , CM000674.1:g.6128575G>A	GRCh37
NC_000012.10:g.5998836G>A	NCBI36
NG_009072.1:g.110262C>T
NG_009072.2:g.110262C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.4009C>T MANE Select	ENSP00000261405.5:p.Pro1337Ser
ENST00000261405.9:c.4009C>T	ENSP00000261405.5:p.Pro1337Ser
ENST00000538635.5:n.421-25475C>T
NM_000552.3:c.4009C>T	NP_000543.2:p.Pro1337Ser
NM_000552.4:c.4009C>T	NP_000543.2:p.Pro1337Ser
NM_000552.5:c.4009C>T MANE Select	NP_000543.3:p.Pro1337Ser